AN IMPROVED PROCESS FOR PREPARING MONTELUKAST AND SALTS THEREOF

Description

[0001] The present invention relates to improved processes for the preparation of Montelukast and its salts thereof.

[0002] Montelukast sodium namely Sodium 1-[[[(1R)-1-[3-[(1E)-2-(7-chloro-2-quinolinyl)ethenyl] phenyl]-3-[2-(1-hydroxy-1-methylethyl) phenyl] propyl] thio] methyl] cyclo propane acetic acid has the formula

[0003] Montelukast sodium is a leukotriene antagonist and inhibits the synthesis of leukotriene biosynthesis. It is useful as anti-asthmatic, anti-allergic, anti-inflammatory, cytoprotective agent and hence useful in the treatment of angina, cerebral spasm, glomerular nephritis, hepatic, end toxemia, uveitis and allograft rejection.

[0004] EP 0 480 717 discloses Montelukast sodium along with other related compounds and the methods for their preparation. The reported method of synthesis proceeds through corresponding methyl ester namely, and involves coupling methyl 1-(mercaptomethyl) cyclopropane acetate with a mesylate generated in-situ. The methyl ester is hydrolyzed to free acids and the latter converted directly to Montelukast sodium salt. The process is not suitable for large-scale production because it requires tedious chromatographic purification of the methyl ester intermediate and /or the final product with low yield.

[0005] U.S. Pat. No. 5,614,632 discloses a process for the preparation of the sodium salt of montelukast and certain process intermediates. The process involves generation of dilithium dianion of 1-(mercaptomethyl) cyclopropaneacetic acid followed by condensation with 2-(2-(3(S)-(3-(2-(7-chloro-2-quinolinyl) ethenyl) phenyl)-3-methanesulfonyloxypropyl) phenyl)-2-propanol (referred as mesylated alcohol) to afford montelukast, which is further converted to the corresponding sodium salt via dicyclohexyl amine salt. The '362 patent also discloses a process for the preparation of crystalline montelukast sodium salt and mesylated alcohol. The process involves reacting methyl 2(3 (S)-(3-(2-(7-chloro-2-quinolinyl) ethenyl) phenyl)-3-hydroxy propyl) benzoate with methyl magnesium chloride to give a diol, which is further converted to mesylated alcohol on reaction with methane sulfonyl chloride. While certain processes of its preparation are known, there is a continuing need for new processes of preparation of Montelukast and its salts. It is mentioned by the inventors of patent U.S. Pat. No. 5,614,632, that the crystalline montelukast dicyclohexylamine salt offers an efficient method for the purification of montelukast, which circumvents the need to use chromatographic purification.

[0006] Processes for preparation of montelukast and its intermediates have also been described in U.S. Patent No's. 5,523,477, and U.S. Patent Application Publication Nos. 2005/0234241, 2005/0256156, 2005/0107612, and International Application Publication Nos. WO 2005/105749, WO 2005/000807, WO 2004/108679, and WO 2006/021974.

[0007] WO 2006/08751 discloses a process for preparation of Montelukast sodium by neutralizing Montelukast organic amine salts such as [alpha]-Methyl benzyl amine salt, diisopropyl amine salt, dibenzyl amine salt followed by treatment with ethanolic sodium hydroxide.

[0008] In the article "Synthesis of Montelukast (MK-0476) Metabolic Oxidation Products" by C. Dufresne et al. in J. Org. Chem. 1996, 61, 8518-8525, it is stated that oxidative metabolites of montelukast by microsomal oxidation in vitro has been described in the prior art, whereby some metabolites have only been tentatively identified. In the article, the chemical synthesis of six oxidized derivatives of montelukast is described, whereby these derivatives should serve as key tools in the identification of the oxidative metabolites of mantelukast.

[0009] Although many processes have been described in the prior art for the preparation of montelukast and its intermediates, there still remains a need for a process for the preparation of montelukast which is industrially viable.

[0010] The main object of the present invention is to provide an improved process for the preparation of Montelukast and its salts thereof.

[0011] Another object of the present invention is to provide novel amine salts of Montelukast.

[0012] Another object of the invention is to provide a process for the preparation of novel amine salts of Montelukast.

[0013] Another object of the present invention is to provide a process for the preparation of Montelukast alkali/alkaline salts using amine salts of Montelukast.

[0014] Another object of the present invention is to provide a process for the preparation of Montelukast alkali/alkaline salts without isolating Montelukast free acid.

[0015] Another object of the present invention is to provide a process for the preparation of Montelukast and its salts which is scalable and economical.

[0016] The present invention is best described with the following synthetic scheme-1;

[0017] In accordance with the present invention the main object is to prepare montelukast and salts thereof comprising the steps of;

a. Optionally treating 2-[2-[3(S)-[3-[2-(7-Chloro-2-quniolinyl)ethenyl]phenyl]-3-hydroxypropyl] phenyl]-2-propanol with acetic anhydride followed by dehydration with PTSA yields (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl) vinyl) phenyl)-3-(2-isopropenyl phenyl] propyl acetate of formula (III)

b. Optionally converting (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl) vinyl) phenyl)-3-(2-isopropenyl phenyl] propyl acetate to (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl) vinyl) phenyl)-3-(2-isopropenyl phenyl] propan-1-ol of formula (IV) (hydroxy styrene)

c. Treating (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl) vinyl) phenyl)-3-(2-isopropenyl phenyl] prapan-1-ol with mesyl chloride or tosyl chloride yields (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-isopropenylphenyl]propyl methane sulphonate or tosylate of formula (V) (mesylated or tosylated styrene)

d. Condensing (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl) vinyl) phenyl)-3-(2-iso propenyl phenyl] propyl methane sulphonate or tosylate with 1-(mercapto methyl) cyclopropane acetic acid followed by salification with an amine gives (1-[(R)-1-(3-[(E)-2-(7-chloroquinolin-2-yl)vinyl]-phenyl)-3-(2-isopropenylphenyl) propylsulfanyl methyl] cyclopropyl] acetic acid amine salt (styrene amine salt) of formula (VI).

e. Converting (1-[(R)-1-(3-[(E)-2-(7-chloroquinolin-2-yl)vinyl]-phenyl)-3-(2-isopropenyl phenyl)propylsulfanylmethyl]cyclopropyl] acetic acid amine salt to montelukast amine salt of formula (VII)

f. Converting Montelukast amine salt to Montelukast free acid or an alkali or alkaline salt thereof.

[0018] In a preferred embodiment, 2-[2-[3(S)-[3-[2-(7-Chloro-2-quniolinyl)ethenyl]phenyl]-3-hydroxypropyl] phenyl]-2-propanol is treated with acetic anhydride followed by dehydration with PTSA yields (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl) phenyl)-3-(2-isopropenyl phenyl]propylacetate of Formula (III). The compound of formula (III) is converted to (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl) vinyl) phenyl)-3-(2-isopropenyl phenyl] propan-1-ol (hydroxy styrene) of Formula (IV)

[0019] The compound of formula (IV) is mesylated with methane sulfonyl chloride or tosylated with toluene sulfonyl chloride to form (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl) vinyl)-phenyl)-3-(2-isopropenylphenyl]propyl ethane sulphonate . (mesylated styrene) of formula (V) or a corresponding tosylate. The reaction may process in polar solvent or non-polar solvent, or in a mixture of polar and non-polar organic solvents. The resulting leaving group containing intermediate (mesylate or tosylate, preferably, mesylate) is then condensed with 1-mercapto methyl cyclopropane acetic acid of formula in the presence of a base. The use of a mixture of polar organic solvents is preferred. The product of this reaction is preferably isolated in the form of an organic amine salt, preferably, dicyclohexyl amine salt of formula (VI).

[0020] The resultant amine salt is reacted with sulphuric acid to get Montelukast free acid and is again converted to its organic amine salt of formula (VII) to get more pure compound. The amine salt of Montelukast of formula (VII) is conveniently converted into alkali/alkaline salts, preferably sodium salt using sodium methoxide or sodium hydroxide.

[0021] In a specific embodiment, the invention provides a process for the preparation of Montelukast and its pharmaceutically acceptable salts, preferably, its sodium salt, which involves:

a) reacting the hydroxy styrene compound with methane sulfonyl chloride in the presence of a tertiary amine, for example, diisopropyl ethyl amine or triethyl amine, in a polar and non-polar or mixture of organic solvents at a temperature of -25 to 50°C.;

b) stirring the reaction mass obtained in step (a) till the reaction substantially completes and subsequently working up the mixture to obtain the mesylated compound of formula (V);

c) reacting the mesylated compound of formula (V) with 1-mercapto methyl cyclopropane acetic acid in polar organic solvents or mixture of polar solvents in the presence of a base, for example, sodium methoxide, sodium ethoxide, sodium hydride, n-butyl lithium, or cesium carbonate preferably 25% sodium methoxide in methanol at a temperature, of -15 to 60°C.;

d) stirring the reaction mass obtained in step (c) till the reaction complies and subsequently working it up to obtain a styrene compound, which is then reacted with dicyclohexyl amine salt to afford the amine salt of formula (VI);

e) treating the dicyclohexyl amine salt of formula (VI) with sulphuric acid wherein the sulphuric acid is either aqueous or concentrated at a temperature of -20 to +50°C.;

f) stirring the reaction mass obtained in step (e) till the reaction complies and subsequently working it up to isolate Montelukast acid and further reacting the resultant montelukast free acid with primary, secondary or tertiary amines, preferably 1-methyl-3-phenylpropylamine, 1,2-cyclohexyl diamine to afford the amine salt of formula (VII);

g) converting the amine salt into its pharmaceutically acceptable salts by generating the Montelukast free acid from montelukast amine salt in halogenated solvents, for example, chloroform, dichloromethane or dichloroethane, preferably, dichloromethane, or an aromatic hydrocarbon, for example toluene in the presence of an organic acid, preferably acetic acid;

h) converting the obtained solution in step (g) to sodium salt of Montelukast using sodium hydroxide, sodium methoxide or sodium ethoxide in alcohols such as from methanol, ethanol, propanol, butanol, 2-propanol or tert butanol, preferably, by using ethanolic sodium hydroxide;

i) distilling the solvent from the reaction solution of step (g) under reduced pressure and;

j) dissolving the above residue in methanol and treating with activated carbon

k) distilling methanol completely and isolating the desired product by adding cyclohexane, n-pentane, n-heptane or hexanes; and

l) drying the isolated solid at 50-95°C. under vacuum.

[0022] The Montelukast sodium obtained in the present novel process is having >99.0% enantiomeric excess purity and resulted in amorphous form. The Montelukast sodium obtained in the present process is also free flowing and non-solvated solid; hence it is well suited for pharmaceutical applications.

[0023] Unless stated to the contrary, any use of the words such as "including," "containing," "comprising," "having" and the like, means "including without limitation" and shall not be construed to limit any general statement that it follows to the specific or similar items or matters immediately following it. Except where the context indicates to the contrary, All exemplary values are intended to be fictitious, unrelated to actual entities and are used for purposes of illustration only. Most of the foregoing alternative embodiments are not mutually exclusive, but may be implemented in various combinations.

Examples:

[0024] The present invention will now be further explained in the following examples. One of ordinary skill in the art will understand how to vary the exemplified preparations to obtain the desired results.

Example - I:

Preparation of (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-(1-hydroxy-1-methylethyl) phenyl]propyl acetate.

[0025] To a stirred solution of 2-[2-[3(S)-[3-[2-(7-Chloro-2-quniolinyl)ethenyl]phenyl]-3-hydroxy propyl]phenyl]-2-propanol (100gm) in dichloromethane (500ml) at 25-30°C 4-di(methyl amino) pyridine (5.32gm) was added and cooled to 0°C. To the reaction mixture Triethylamine (26.4gm) was added at 0°C. Acetic anhydride (26.7gm) was added slowly at temp.0-5°C over 30-60 min and maintained the reaction at temp. 0-5°C over 30 min. Reaction completion was monitored by TLC. After reaction completion the reaction mass was quenched into 7% NaHCO₃(500ml) and stirred for 15min.Temperature was raised to 25-30°C and maintained for 30 min. Reaction mass was settled for 15 min and separated the organic layer. Aq.layer was extracted with dichloromethane (250ml). The combined organic layer was washed with 25% NH₄Cl solution (500ml). Organic layer was distilled below 40°C to get the desired product as residue.
Output: 108.0 gm

Example - II:

Preparation of (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl) vinyl) phenyl)-3-(2-isopropenyl phenyl] propyl acetate

[0026] PTSA (62.4gm) was suspended in toluene (300ml) at 25-30°C and moisture was removed by azeotropic distillation. After removal of moisture reaction mass was cooled to 70°C and distilled toluene completely under reduced pressure to get residue. The obtained residue was cooled to room temperature and charged dichloromethane (300ml) and stage-I (108gm of stage-I dissolved in 200ml dichloromethane). The reaction mass temp was raised to reflux and maintained for 2 hrs. Reaction completion was monitored by TLC. After reaction completion the reaction mass was quenched into 7% NaHCO₃ (300ml) and stirred for 15min. Reaction mass temp was raised to 25-30°C and maintained for 30 min. Reaction mass was settled for 15 min and the organic layer was separated. Aq.layer was extracted with dichloromethane (200ml) at 25-30°C. The combined organic layer was washed with of DM Water (2x300ml). Organic layer was concentrated below 40°C to get the desired product as residue.
Output: 101.2 gm

Example - III:

Preparation of (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl) vinyl) phenyl)-3-(2-isopropenyl phenyl] propan-1-ol HCl

[0027] To a stirred solution of Stage-II (101 gm) in methanol (500ml) NaOH solution (35gm of NaOH dissolved in 52ml DM Water) was added at 25-30°C over 30 min. Reaction completion was checked by TLC. After reaction completion methanol and water were completely distilled under reduced pressure below 50°C. The residue was dissolved in ethyl acetate (600ml). To the obtained solution DM water (500ml) was added pH was adjusted to 6.5-7.0 slowly with 1:1 dil HCl at 25-30°C. Aq layer was separated and again extracted with ethyl acetate (200ml). The combined organic layer was washed with DM Water (500ml). The separated organic layer was dried over sodium sulphate and concentrated completely under reduced pressure at temp below 45°C. The obtained residue was dissolved in methanol (300ml) and methanolic HCl (80ml of 8%) was added over 30-60 min at room temperature. Reaction mixture was maintained for 2 hrs at room temperature one hour at 10-15°C. The precipitated product was filtered and washed the wet cake with chilled methanol (50ml).
Output: 88.0 gm

Example - IV:

Preparation of (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-iso propenyl phenyl] propyl methane sulphonate

[0028] To a stirred solution of compound obtained in Example-III (100gm) in dichloromethane (600ml), DM water (300ml) was charged and pH was adjusted to 7.5 to 8.0 with ammonia solution at 25-30°C. Reaction mass was stirred for 30 min at 25-30°C and settled for 10 min. Organic layer was separated and the aq.layer was extracted with dichloromethane(200ml). The combined organic layer was washed with DM Water (2x300ml). Dichloromethane was distilled completely below 40°C to get residue. The obtained residue was dissolved in dichloromethane (600ml) and cooled to 0°C. Di isopropyl ethyl amine (DIPEA) (40.6gm) was added under N₂ atmosphere and again cooled to -30°C. Methane sulphonyl chloride (31.33gm) was added at -30 to -25°C slowly over 60 min and maintained the reaction at -30° to -25°C for 2 hrs under N₂ atmosphere. Reaction completion was checked by TLC. After reaction completion, the reaction mass was quenched in to 7% NaHCO₃ (1000ml) below 5°C. The reaction mass was maintained for 10 min at 0-5°C and 30 min at 25-30°C. Organic layer was separated and aq.layer was extracted with dichloromethane (200ml).The combined organic layer was washed with DM water (2x500ml). Dichloromethane was distilled out completely below 40°C to get desired product as residue.
Output: 105.0 gm

Example - V:

Preparation of (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl) vinyl) phenyl)-3-(2-iso propenyl phenyl] propyl methane sulphonate

[0029] To a stirred solution of Stage-III (100gm) in dichloromethane (300ml) Diisopropylethylamine (27.1 gm) was charged and Reaction mass was stirred for 30 min at 40-45°C. Dichloromethane was distilled completely below 40°C to get residue. The obtained residue was dissolved in dichloromethane (1000ml) and cooled to 0°C. Di isopropyl ethyl amine (DIPEA) (40.6gm) was added under N₂ atmosphere and again cooled to 0°C. Methane sulphonyl chloride (31.33gm) was added at 0 to 5°C slowly over 60 min and maintained the reaction at 0° to 5°C for 2 hrs under N₂ atmosphere. Reaction completion was checked by TLC. After reaction completion, the reaction mass was quenched in to 7% NaHCO₃ (1000ml) below 5°C. The reaction mass was maintained for 10 min at 0-5°C and 30 min at 25-30°C. Organic layer was separated and aq.layer was extracted with dichloromethane (200ml).The combined organic layer was washed with DM water (2x500ml). Dichloromethane was distilled out completely below 40°C to get desired product as residue.
Output: 105.0 gm

Example - VI:

Preparation of DCHA salt of (1-[(R)-1-(3-[(E)-2-(7-chloroquinolin-2-yl) vinyl]-phenyl)-3-(2-isopropenylphenyl) propylsulfanylmethyl] cyclopropyl] acetic acid (Styrene DCHA salt)

[0030] To a stirred solution of 1-(mercapto methyl) cyclopropane acetic acid (46gm) in DMF (300ml), NaH (25gm) was added in four equal lots over 60 min at -5 - 0°C. The reaction mixture was maintained for 2 hrs at -5 - 0°C. Stage-IV (100gm dissolves in 300ml of DMF) was added at -5 - 0°C over 1 hr. The reaction mixture was maintained at 0-5°C for 15 hrs. The reaction completion was checked by TLC. After reaction completion reaction mixture was quenched in to mixture of 10% NaCl (1000ml), and ethyl acetate (1000ml) below 10°C. Reaction mixture was stirred for 10 min at 0-10°C and 30 min at room temperature. Organic layer was separated and the aq.layer was extracted with ethyl acetate (500 ml). The combined organic layer was washed with 5% tartaric acid solution (500ml) followed by of DM Water (2x500ml). Separated organic layer was dried over 25 g of Sodium sulphate. Ethyl acetate was distilled completely under reduced pressure below 45°C. The obtained residue was dissolved in ethyl acetate (600ml) at room temperature. To the above solution dicyclohexyl amine (50ml) was added at room temperature over 30 min under nitrogen atmosphere. Reaction mixture was maintained for 1 hr at room temperature and seeded with pure dicyclohexyl amine salt. Reaction mixture was maintained for 12-24 hrs at room temperature. n-Hexane (1200ml) was added slowly at room temperature over 60 min and maintained for 12 hrs. The precipitated product is filtered and washed with of n-Hexane (200ml).
Output: 100.0 gm

Example - VII:

Preparation of DCHA salt of (1-[(R)-1-(3-[(E)-2-(7-chloroguinolin-2-yl)vinyl]-phenyl)-3-(2-isopropenylphenyl) propylsulfanylmethyl] cyclopropyl] acetic acid (Styrene DCHA salt)

[0031] To a stirred solution of 1-(mercapto methyl) cyclopropane acetic acid (36.7 gm) in DMF (300ml), sodium methoxide (108.6 gm 25% methanolic soln) was added over 60 min at 0-5°C. The reaction mixture was maintained for 2 hrs at 0-5°C. mesylated Styrene (100gm dissolves in 300ml of DMF) was added at 0-5°C over 1 hr. The reaction mixture was maintained at 0-5°C for 15 hrs. The reaction completion was checked by TLC. After reaction completion reaction mixture was quenched in to mixture of 10% NaCl (1000ml), and ethyl acetate (1000ml) below 10°C. Reaction mixture was stirred for 10 min at 0-10°C and 30 min at room temperature. Organic layer was separated and the aq.layer was extracted with ethyl acetate (500 ml). The combined organic layer was washed with 5% tartaric acid solution (500ml) followed by of DM Water (2x500ml). Separated organic layer was dried over 25 g of Sodium sulphate. Ethyl acetate was distilled completely under reduced pressure below 45°C. The obtained residue was dissolved in ethyl acetate (600ml) at room temperature. To the above solution dicyclohexyl amine (50ml) was added at room temperature over 30 min under nitrogen atmosphere. Reaction mixture was maintained for 1 hr at room temperature and seeded with pure dicyclohexyl amine salt. Reaction mixture was maintained for 12-24 hrs at room temperature. n-Hexane (1200ml) was added slowly at room temperature over 60 min and maintained for 12 hrs. The precipitated product is filtered and washed with of n-Hexane (200ml).
Output: 101.0 gm

Example - VIII: Preparation of Montelukast amine salt

[0032] To a stirred solution of Styrene DCHA salt (100gm) in dichloromethane (500ml) to DM Water (300ml) was charged and pH was adjusted 4.0 to 4.5 with 1:1 dil Acetic acid at 25-30°C. The reaction mixture was stirred for stirred for 30 min at room temperature. Organic layer was separated and aq.layer was extracted with dichloromethane (300ml). The combined organic layer was washed with DM water (2x300ml). Organic layer was concentrated under below 40°C to get semi solid material. n-Hexane (500ml) was added and stirred for 30 min at room temperature. The precipitate was filtered and washed the wet cake with n-Hexane (100ml).The wet product was dried at 40-45°C to get styrene free acid (73gm).

[0033] Styrene free acid (73gm) was added to sulfuric acid (365ml of 80%) in equal lots at 5°-10°C. Reaction mass was maintained for 1 hr at 5-10°C. Reaction completion was monitored by TLC. After the reaction completion (product is ~65%, styrene is ~30%) the reaction mass was quenched into a mixture of DM water (730ml),ethyl acetate (730ml) and t-butanol (730ml) below 10°C. After quenching the reaction mass pH was adjusted to 3.5-4.0 with 20% NaOH below10°C. Again the temperature was raised to 25-30°C and maintained for 30 min. Organic layer was separated and aq. layer was extracted with ethyl acetate (2x730ml) at room temperature. The combined organic layer was washed with DM water (2x730ml). The organic layer was over sodium sulphate and concentrated under reduced pressure below 45°C to get the desired product as residue. The obtained residue was subjected to column chromatography (Mobile phase is dichloromethane: methanol, 99.5: 0.5). The separated montelukast free acid was dissolved in ethyl acetate (180ml) at 40°C and cooled to room temperature under N₂ atmosphere.

[0034] To the obtained solution 1-methyl-3-phenylpropylamine (9.7ml) was added slowly at 25-30°C over 30 min.Reaction mass was maintained for 60 min, seeded and maintain for 12-16 hrs at 25-30°C under N₂ atmosphere. After the product was precipitated, n-Hexane (360ml) was added slowly over 1 hr at 25-30°C. The reaction mass was maintained at 25-30°C for 12 hrs. The precipitated product was filtered and washed the wet cake with n-Hexane (60ml). The wet product was dried at 45-50°C. The dried product was purified by recrystallization in toluene.
Output: 70.0gm

Example - IX: Preparation of Montelukast amine salt

[0035] To sulfuric acid (500 ml of 80%) styrene DCHA salt (100 gm) was added in equal lots at 5°-10°C. Reaction mass was maintained for 1 hr at 5-10°C. Reaction completion was monitored by HPLC. After the reaction completion the reaction mass was quenched into a mixture of DM water (1000ml),ethyl acetate (1000ml) and t-butanol (1000ml) below 10°C. After quenching the reaction mass pH was adjusted to 3.5-4.0 with 20% NaOH belowl0°C. Again the temperature was raised to 25-30°C and maintained for 30 min. Organic layer was separated and aq. layer was extracted with ethyl acetate (2x500ml) at room temperature. The combined organic layer was washed with 5% brine (2x1000ml). The organic layer was over sodium sulphate and concentrated under reduced pressure below 45°C to get the desired product as residue. The obtained residue was subjected to column chromatography (Mobile phase is dichloromethane: methanol, 99.5: 0.5). The separated montelukast free acid was dissolved in ethyl acetate (300ml) at 40°C and cooled to room temperature under N₂ atmosphere.

[0036] To the obtained solution 1-methyl-3-phenylpropylamine (16.2ml) was added slowly at 25-30°C over 30 min. Reaction mass was maintained for 60 min, seeded and maintain for 12-16 hrs at 25-30°C under N₂ atmosphere. After the product was precipitated, n-Hexane (600ml) was added slowly over 1 hr at 25-30°C. The reaction mass was maintained at 25-30°C for 12 hrs. The precipitated product was filtered and washed the wet cake with n-Hexane (100ml). The wet product was dried at 45-50°C. The dried product was purified by recrystallization in toluene.
Output: 50.0gm
Purity by HPLC: 98.2%

Example - X: Preparation of Montelukast sodium salt

[0037] To a suspension of Montelukast 1-methyl-3-phenylpropylamine salt (100gm) in dichloromethane (2000ml) DM water (1000ml) was charged pH was adjusted to 4.0 to 4.5 with acetic acid (1:1) at 25-30°C. Reaction mass was maintained at 25-30°C for 30 min and settle for 20 min. Organic layer was separated and aq.layer was extracted with dichloromethane (1000ml). The combined organic layer was washed with DM Water (1000 ml). To the organic layer ethanolic NaOH solution (235 ml of ethanol, 2.1 ml of DM Water and 5.17 g of NaOH) was slowly added over 30 min and maintained at 25-30°C for 30 min. Dichloromethane was distilled completely below 40°C to get semi solid material. Then methanol (800 ml) was charged at 40-45°C under N₂ atmosphere and stirred for 10 min. The obtained clear solution was treated with activated carbon and filtered the mass over hyflo bed and washed with methanol (200ml). The clear filtrate was distilled out completely under reduced pressure below 45°C. Pentane (100ml) was charged to the above residue and distilled out methanol traces completely below 45°C. Again Pentane (2000ml) was and maintained for 4 hrs at 25-30°C under N₂ atmosphere. The precipitated product was filtered under N₂ atmosphere and washed the wet cake with Pentane (100ml). The obtained wet cake was dried under vacuum for 2 hrs at 50°C, 2 hr at 70-75°C finally at 85-95°C for 24 hrs.
Output: 70.0 gm
HPLC Purity: 99.5%

Claims

1. A process for preparation of Montelukast or a salt thereof, said process comprising the steps of:

a. reacting (S)-1-(3-((E)-2-(7-chloroquinolin-2-yl) vinyl) phenyl)-3-(2-isopropenyl phenyl]propan-1-ol with methane sulfonyl chloride or toluene sulfonyl chloride to obtain the mesylated or tosylated derivative (styrene mesylate or styrene tosylate);

b. condensing the styrene mesylate or styrene tosylate with 1-(mercapto methyl) cyclopropane acetic acid followed by saltification with an amine to obtain (1-[(R)-1-(3-[(E)-2-(7-chloroquinolin-2-yl)vinyl]-phenyl)-3-(2-isopropenylphenyl) propylsulfanyl methyl] cyclopropyl]acetic acid amine salt (styrene amine salt);

c. converting the styrene amine salt to Montelukast amine salt; and

d. converting the Montelukast amine salt to Montelukast free acid or alkali or an alkaline salt thereof.

2. The process of claim 1, wherein the reaction step (a) is carried out in the presence of an organic solvent selected from chlorinated hydrocarbons, aromatic hydrocarbons, Tetrahydrofuran and mixtures thereof.

3. The process of claim 1, wherein the reaction step (b) is carried out in a polar solvent in the presence of a base.

4. The process of claim 3, wherein said polar solvent is selected from N,N-dimethylformamide, dimethylsulphoxide, N,N-dimethylacetamide, N-methylpyrrolidine, methanol, THF and mixtures thereof.

5. The process of claim 3, wherein said base is selected from metal alkoxides, metal hydrides, metal carbonates, alkyl lithium salts and mixtures thereof.

6. The process of claim 1, wherein the amine in reaction step (b) is dicyclohexylamine.

7. The process of claim 1, wherein the reaction step (c) includes treating said styrene amine salt with sulphuric acid and isolating the obtained Montelukast as amine salt.

8. The process of claim 1, wherein the reaction step (c) includes converting said styrene amine salt to its free acid, treating said free acid with sulphuric acid and isolating the obtained Montelukast as amine salt.

9. The process of claim 1, wherein said Montelukast amine salt is selected from 1-methyl-3-phenylpropylamine, 1,2-cyclohexyl diamine salt and mixtures thereof.

10. The process of claim 1, wherein the reaction step (d) includes converting said Montelukast amine salt to its free acid, treating said free acid with an alkali or alkaline base and isolating Montelukast as alkali or alkaline salt.

11. The process of claim 10, wherein the reaction step (d) includes (i) providing a solution of Montelukast free acid in a halogenated solvent, aromatic solvent, alkanols or mixtures thereof; (ii) treating said solution with an alcoholic base to convert said Montelukast free acid into an alkali or alkaline salt of Montelukast; (iii) concentrating the reaction mass to dryness; (iv) adding a cyclic or acyclic hydrocarbon solvent to the residue thereby precipitating said alkali or alkaline salt of Montelukast.

12. The process of claim 1, wherein the reaction step (d) includes treating the Montelukast amine salt with an alkali or alkaline base and isolating Montelukast as an alkali or alkaline salt.

13. The process of claim 12, wherein the reaction step (d) includes (i) providing a solution of Montelukast amine salt in a halogenated solvent, aromatic solvent, or mixtures thereof; (ii) treating said solution with an alkali or alkaline base to convert said Montelukast amine salt into a salt of Montelukast; (iii) concentrating the reaction mass to dryness; (iv) adding a cyclic or acyclic hydrocarbon solvent to the residue thereby precipitating said alkali or alkaline salt of Montelukast.

14. The process of claim 13, wherein said alkali or alkaline base is selected from sodium hydroxide, sodium methoxide and sodium ethoxide in methanol, ethanol, propanol, butanol, 2-propanol or tert-butanol.

15. The process of claim 11 or 13, wherein said hydrocarbon solvent is selected from cyclohexane, pentane, hexane, heptane and mixtures thereof.

16. The use of anyone of the following compounds:

(S)-1-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-isopropenylphenyl)propyl acetate,

(S)-1-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-isopropenylphenyl)propan-1-ol,

(S)-1-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-isopropenylphenyl)propyl mesylate,

(S)-1-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-isopropenylphenyl)propyl tosylate, and

(1-((R)-1-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-isopropenylphenyl)propylsulfanylmethyl)cyclopropyl) acetic acid amine salt for the preparation of Montelukast or a salt thereof.

Ansprüche

1. Verfahren zur Herstellung von Montelukast oder eines Salzes davon, wobei das Verfahren die Schritte umfasst:

a. Umsetzen von (S)-1-(3-((E)-2-(7-Chiorchinolin-2-yl)vinyl)phenyl)-3-(2-isopropenylphenyl]propan-1-ol mit Methansulfonylchlorid oder Toluensulfonylchlorid, um das mesylierte oder tosylierte Derivat (Styrolmesylat oder Styroltosylat) zu erhalten;

b. Kondensieren des Styrolmesylats oder Styroltosylats mit 1-(Mercaptomethyl)cyclopropanessigsäure gefolgt von Salzbildung mit einem Amin, um (1-[(R)-1-(3-[(E)-2-(7-Chlorchinolin-2-yl)vinyl]phenyl)-3-(2-isopropenylphenyl)propylsulfanylmethyl]cyclopropyl]essigsäure-Aminsalz (Styrol Aminsalz) zu erhalten;

c. Umwandlung des Styrol Aminsalzes in das Montelukast Aminsalz; und

d. Umwandlung des Montelukast Aminsalzes in Montelukast freie Säure oder in ein Alkali- oder Erdalkalisalz davon.

2. Verfahren gemäß Anspruch 1, wobei Reaktionsschritt (a) in Gegenwart eines organischen Lösungsmittels, ausgewählt aus chlorierten Kohlenwasserstoffen, aromatischen Kohlenwasserstoffen, Tetrahydrofuran und Mischungen davon, durchgeführt wird.

3. Verfahren gemäß Anspruch 1, wobei Reaktionsschritt (b) in einem polaren Lösungsmittel in Gegenwart einer Base durchgeführt wird.

4. Verfahren gemäß Anspruch 3, wobei das polare Lösungsmittel aus N,N-Dimethylformamid, Dimethylsulfoxid, N,N-Dimethylacetamid, N-Methylpyrrolidin, Methanol, THF und Mischungen davon ausgewählt ist.

5. Verfahren gemäß Anspruch 3, wobei die Base aus Metallalkoxiden, Metallhydriden, Metallcarbonaten, Alkyllithiumsalzen und Mischungen davon ausgewählt ist.

6. Verfahren gemäß Anspruch 1, wobei das Amin im Reaktionsschritt (b) Dicyclohexylamin ist.

7. Verfahren gemäß Anspruch 1, wobei Reaktionsschritt (c) die Behandlung des Styrol Aminsalzes mit Schwefelsäure und die Isolierung des erhaltenen Montelukastes als Aminsalz umfasst.

8. Verfahren gemäß Anspruch 1, wobei Reaktionsschritt (c) die Umwandlung des Styrol Aminsalzes in seine freie Säure, die Behandlung der freien Säure mit Schwefelsäure und die Isolierung des erhaltenen Montelukastes als Aminsalz umfasst.

9. Verfahren gemäß Anspruch 1, wobei das Montelukast Aminsalz aus 1-Methyl-3-phenylpropylaminsalz, 1,2-Cyclohexyldiaminsalz und Mischungen davon ausgewählt ist.

10. Verfahren gemäß Anspruch 1, wobei Reaktionsschritt (d) die Umwandlung des Montelukast Aminsalzes in seine freie Säure, die Behandlung der freien Säure mit Alkali- oder Erdalkali-Base und die Isolierung von Montelukast als Alkali- oder Erdalkalisalz umfasst.

11. Verfahren gemäß Anspruch 10, wobei Reaktionsschritt (d) umfasst: (i) Bereitstellung einer Lösung von Montelukast als freie Säure in einem halogenierten Lösungsmittel, aromatischen Lösungsmittel, Alkanolen oder Mischungen davon; (ii) Behandlung dieser Lösung mit einer alkoholischen Base, um die Montelukast freie Säure in ein Alkali- oder Erdalkalisalz von Montelukast zu überführen; (iii) Konzentration der Reaktionsmasse bis zur Trockne; (iv) Zugabe eines cyclischen oder acyclischen Kohlenwasserstofflösungsmittels zu dem Rückstand, um das Alkali- oder Erdalkalisalz von Montelukast auszufällen.

12. Verfahren gemäß Anspruch 1, wobei Reaktionsschritt (d) die Behandlung des Montelukast Aminsalzes mit einer Alkali- oder Erdalkalibase und die Isolierung des Montelukastes als Alkali- oder Erdalkalisalz umfasst.

13. Verfahren gemäß Anspruch 12, wobei Reaktionsschritt (d) umfasst.: (i) Bereitstellung einer Lösung von Montelukast Aminsalz in einem halogenierten Lösungsmittel, aromatischen Lösungsmittel oder Mischungen davon; (ii) Behandlung dieser Lösung mit einer Alkali- oder Erdalkalibase, um das Montelukast Aminsalz in ein Montelukast Salz zu überführen; (iii) Konzentration der Reaktionsmasse bis zur Trockne; (iv) Zugabe eines cyclischen oder acyclischen Kohlenwasserstofflösungsmittels zu dem Rückstand, um das Alkali- oder Erdalkalisalz von Montelukast auszufällen.

14. Verfahren gemäß Anspruch 13, wobei die Alkali- oder Erdalkalibase aus Natriumhydroxid, Natriummethoxid und Natriumethoxid in Methanol, Ethanol, Propanol, Butanol, 2-Propanol oder tert-Butanol ausgewählt ist.

15. Verfahren gemäß Anspruch 11 oder 13, wobei das Kohlenwasserstofflösungsmittel aus Cyclohexan, Pentan, Hexan, Heptan und Mischungen davon ausgewählt ist.

16. Verwendung einer der folgenden Verbindungen:

(S)-1-(3-((E)-2-(7-Chlorchinolin-2-yl)vinyl)phenyl)-3-(2-isopropenylphenyl)propyl acetat,

(S)-1-(3-((E)-2-(7-Chlorchinolin-2-yl)vinyl)phenyl)-3-(2-isopropenylphenyl)propan-1-ol,

(S)-1-(3-((E)-2-(7-Chlorchinolin-2-yl)vinyl)phenyl)-3-(2-isopopenylphenyl)propylmesylat

(S)-1-(3-((E)-2-(7-Chlorchinolin-2-yl)vinyl)phenyl)-3-(2-isopropenylphenyl)propyltosylat und

(1-((R)-1-(3-((E)-2-(7-Chlorchinolin-2-yl)vinyl)phenyl)-3-(2-isopropenylphenyl)propylsulfanylmethyl)cyclopropyl)essigsäure-Aminsalz

für die Herstellung von Montelukast oder einem Salz davon.

Revendications

1. Procédé pour la préparation du Montélukast ou un sel de celui-ci, ledit procédé comprenant les étapes de :

a. réaction du (S)-1-(3-((E)-2-(7-chloroquinoline-2-yl)vinyl)phényl)-3-(2-isopropénylphényle)propane-1-ol avec du chlorure de méthane sulfonyle ou du chlorure de toluène sulfonyle afin d'obtenir le dérivé mésylate ou tosylate (mésylate de styrène ou tosylate de styrène);

b. condensation du mésylate de styrène ou du tosylate de styrène avec de l'acide 1-(mercapto méthyl) cyclopropane acétique suivie par la salification avec une amine afin d'obtenir du sel d'amine d'acide (1-((R)-1-(3-((E)-2-(7-chloroquinoline-2-yl)vinyl)-phenyl)-3-(2-isopropenylphényle)propylsulfanylméthyl)cyclopropyl) acétique (sel d'amine de styrène);

c. conversion du sel d'amine de styrène en sel d'amine de Montélukast; et

d. conversion du sel d'amine de Montélukast en acide libre de Montélukast ou en son sel alcalin ou alcalino-terreux.

2. Procédé selon la revendication 1 où l'étape de réaction (a) est réalisée en présence d'un solvant organique choisi parmi les hydrocarbures chlorés, les hydrocarbures aromatiques, le tétrahydrofurane et des mélanges de ceux-ci.

3. Procédé selon la revendication 1 où l'étape de réaction (b) est effectuée dans un solvant polaire en présence d'une base.

4. Procédé selon la revendication 3 où ledit solvant polaire est choisi parmi le N,N-diméthylformamide, diméthylsulphoxide, N,N-diméthylacétamide, N-méthylpyrrolidine, méthanol, THF et des mélanges de ceux-ci.

5. Procédé selon la revendication 3 où ladite base est choisie parmi les alcoxydes métalliques, hydrures métalliques, carbonates métalliques, sels de lithium d'alkyle et des mélanges de ceux-ci,

6. Procédé selon la revendication 1 où l'amine dans l'étape de réaction (b) est la dicyclohexylamine.

7. Procédé selon la revendication 1 où l'étape de réaction (c) comprend le traitement dudit sel d'amine de styrène avec de l'acide sulfurique et l'isolement du Montélukast obtenu en tant que sel d'amine.

8. Procédé selon la revendication 1 où l'étape de réaction (c) comprend la conversion dudit sel d'amine de styrène dans son acide libre, le traitement dudit acide libre avec de l'acide sulfurique et l'isolement du Montélukast obtenu en tant que sel d'amine.

9. Procédé selon la revendication 1 où ledit sel d'amine de Montélukast est choisi parmi le sel de 1-méthyl-3-phénylpropylamine, le sel de 1,2-cyclohexyl diamine et des mélanges de ceux-ci.

10. Procédé selon la revendication 1 où l'étape de réaction (d) comprend la conversion dudit sel d'amine de Montélukast dans son acide libre, le traitement dudit acide libre avec une base alcaline ou alcalino-terreuse et l'isolement du Montélukast en tant que sel alcalin ou alcalino-terreux.

11. Procédé selon la revendication 10 où l'étape de réaction (d) comprend: (i) fournir une solution d'acide libre de Montélukast dans un solvant halogéné, un solvant aromatique, des alcanols ou des mélanges de ceux-ci; (ii) traitement de ladite solution avec une base alcoolique afin de convertir ledit acide libre de Montélukast en un sel alcalin ou alcalino-terreux de Montélukast; (iii) concentration de la masse réactionnelle jusqu'à dessiccation; (iv) addition d'un solvant hydrocarbure cyclique ou acyclique au résidu, précipitant ainsi ledit sel alcalin ou alcalino-terreux de Montélukast.

12. Procédé selon la revendication 1 où l'étape de réaction (d) comprend le traitement du sel d'amine de Montélukast avec une base alcaline ou alcalino-terreuse et l'isolement du Montélukast en tant qu'en sel alcalin ou alcalino-terreux.

13. Procédé selon la revendication 12 où l'étape de réaction (d) comprend: (i) fournir une solution de sel d'amine de Montélukast dans un solvant halogéné, un solvant aromatique, ou des mélanges de ceux-ci; (ii) traitement de ladite solution avec une base alcaline ou alcalino-terreuse afin de convertir ledit sel d'amine de Montélukast en un sel de Montélukast; (iii) concentration de la masse réactionnelle jusqu'à dessiccation; (iv) addition d'un solvant hydrocarbure cyclique ou acyclique au résidu, afin de précipiter ledit sel alcalin ou alcalino-terreux de Montélukast.

14. Procédé selon la revendication 13 où ladite base alcaline ou alcalino-terreuse est choisie parmi le sodium hydroxide, le sodium méthoxide et le sodium éthoxide dans du méthanol, éthanol, propanol, butanol, 2-propanol ou tert-butanol.

15. Procédé selon la revendication 11 ou 13 où ledit solvant hydrocarbure est choisi parmi le cyclohexane, pentane, hexane, heptane et des mélanges de ceux-ci.

16. Utilisation de l'un des composés suivants :

(S)-1-(3-((E)-2-(7 -chloroquinoline-2-yl)vinyl)phényl)-3-(2-isopropénylphényle)propyl acétate,

(S)-1-(3-((E)-2-(7-chloroquinoline-2-yl)vinyljphényl)-3-(2-isopropénylphényle)propan-1-ol,

(S)-1-(3-((E)-2-(7-chloroquinoline-2-yl)vinyl)phényl)-3-(2-isopropénylphényle)propyl mésylate,

(S)-1-(3-((E)-2-(7-chloroquinoline-2-yl)vinyl)phényl)-3-(2-isopropénylphényle)propyl tosylate et

le sel d'amine d'acide (1-((R)-1-(3-((E)-2-(7-chloroquinoline-2-yl)vinyl)phényl)-3-(2-isopropénylphényle)propylsulfanylméthyl)cyclopropyl) acétique

pour la préparation du Montélukast ou un sel de celui-ci.